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A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons
Climbing over chasms larger than step size is vital to fruit flies, since foraging and mating are achieved while walking. Flies avoid futile climbing attempts by processing parallax-motion vision to estimate gap width. To identify neuronal substrates of climbing control, we screened a large collecti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891706/ https://www.ncbi.nlm.nih.gov/pubmed/27255169 http://dx.doi.org/10.1038/srep27000 |
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author | Triphan, Tilman Nern, Aljoscha Roberts, Sonia F. Korff, Wyatt Naiman, Daniel Q. Strauss, Roland |
author_facet | Triphan, Tilman Nern, Aljoscha Roberts, Sonia F. Korff, Wyatt Naiman, Daniel Q. Strauss, Roland |
author_sort | Triphan, Tilman |
collection | PubMed |
description | Climbing over chasms larger than step size is vital to fruit flies, since foraging and mating are achieved while walking. Flies avoid futile climbing attempts by processing parallax-motion vision to estimate gap width. To identify neuronal substrates of climbing control, we screened a large collection of fly lines with temporarily inactivated neuronal populations in a novel high-throughput assay described here. The observed climbing phenotypes were classified; lines in each group are reported. Selected lines were further analysed by high-resolution video cinematography. One striking class of flies attempts to climb chasms of unsurmountable width; expression analysis guided us to C2 optic-lobe interneurons. Inactivation of C2 or the closely related C3 neurons with highly specific intersectional driver lines consistently reproduced hyperactive climbing whereas strong or weak artificial depolarization of C2/C3 neurons strongly or mildly decreased climbing frequency. Contrast-manipulation experiments support our conclusion that C2/C3 neurons are part of the distance-evaluation system. |
format | Online Article Text |
id | pubmed-4891706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48917062016-06-10 A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons Triphan, Tilman Nern, Aljoscha Roberts, Sonia F. Korff, Wyatt Naiman, Daniel Q. Strauss, Roland Sci Rep Article Climbing over chasms larger than step size is vital to fruit flies, since foraging and mating are achieved while walking. Flies avoid futile climbing attempts by processing parallax-motion vision to estimate gap width. To identify neuronal substrates of climbing control, we screened a large collection of fly lines with temporarily inactivated neuronal populations in a novel high-throughput assay described here. The observed climbing phenotypes were classified; lines in each group are reported. Selected lines were further analysed by high-resolution video cinematography. One striking class of flies attempts to climb chasms of unsurmountable width; expression analysis guided us to C2 optic-lobe interneurons. Inactivation of C2 or the closely related C3 neurons with highly specific intersectional driver lines consistently reproduced hyperactive climbing whereas strong or weak artificial depolarization of C2/C3 neurons strongly or mildly decreased climbing frequency. Contrast-manipulation experiments support our conclusion that C2/C3 neurons are part of the distance-evaluation system. Nature Publishing Group 2016-06-03 /pmc/articles/PMC4891706/ /pubmed/27255169 http://dx.doi.org/10.1038/srep27000 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Triphan, Tilman Nern, Aljoscha Roberts, Sonia F. Korff, Wyatt Naiman, Daniel Q. Strauss, Roland A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons |
title | A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons |
title_full | A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons |
title_fullStr | A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons |
title_full_unstemmed | A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons |
title_short | A screen for constituents of motor control and decision making in Drosophila reveals visual distance-estimation neurons |
title_sort | screen for constituents of motor control and decision making in drosophila reveals visual distance-estimation neurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4891706/ https://www.ncbi.nlm.nih.gov/pubmed/27255169 http://dx.doi.org/10.1038/srep27000 |
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